AU2002222682B8 - Tropolone Derivatives - Google Patents

Tropolone Derivatives Download PDF

Info

Publication number
AU2002222682B8
AU2002222682B8 AU2002222682A AU2002222682A AU2002222682B8 AU 2002222682 B8 AU2002222682 B8 AU 2002222682B8 AU 2002222682 A AU2002222682 A AU 2002222682A AU 2002222682 A AU2002222682 A AU 2002222682A AU 2002222682 B8 AU2002222682 B8 AU 2002222682B8
Authority
AU
Australia
Prior art keywords
group
hydrogen atom
mmol
mhz
nmr
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
AU2002222682A
Other versions
AU2002222682B2 (en
AU2002222682A1 (en
Inventor
Hiroyuki Kagechika
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
RESEARCH FOUNDATION ITSUU LABORATORY
Original Assignee
Res Foundation Itsuu Laboratory
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Res Foundation Itsuu Laboratory filed Critical Res Foundation Itsuu Laboratory
Publication of AU2002222682A1 publication Critical patent/AU2002222682A1/en
Assigned to RESEARCH FOUNDATION ITSUU LABORATORY reassignment RESEARCH FOUNDATION ITSUU LABORATORY Request for Assignment Assignors: KAGECHIKA, HIROYUKI, RESEARCH FOUNDATION ITSUU LABORATORY
Publication of AU2002222682B2 publication Critical patent/AU2002222682B2/en
Application granted granted Critical
Publication of AU2002222682B8 publication Critical patent/AU2002222682B8/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/50Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D333/74Naphthothiophenes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/30Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms
    • C07C233/33Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/02Nutrients, e.g. vitamins, minerals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/26Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
    • C07C17/263Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
    • C07C17/266Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions of hydrocarbons and halogenated hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C225/00Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
    • C07C225/20Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C225/00Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
    • C07C225/22Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/30Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms
    • C07C233/32Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/64Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C233/76Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C245/00Compounds containing chains of at least two nitrogen atoms with at least one nitrogen-to-nitrogen multiple bond
    • C07C245/02Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides
    • C07C245/06Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides with nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings
    • C07C245/10Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides with nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings with nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/28Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/28Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C275/38Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by doubly-bound oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/20Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/62Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by hydrogenation of carbon-to-carbon double or triple bonds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/63Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by introduction of halogen; by substitution of halogen atoms by other halogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/64Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by introduction of functional groups containing oxygen only in singly bound form
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/65Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/673Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by change of size of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/70Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form
    • C07C45/71Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form being hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/657Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings
    • C07C49/683Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings having unsaturation outside the aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/703Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups
    • C07C49/747Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups containing six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/753Unsaturated compounds containing a keto groups being part of a ring containing ether groups, groups, groups, or groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/38Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/40Radicals substituted by oxygen atoms
    • C07D307/46Doubly bound oxygen atoms, or two oxygen atoms singly bound to the same carbon atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/22Radicals substituted by doubly bound hetero atoms, or by two hetero atoms other than halogen singly bound to the same carbon atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/18Systems containing only non-condensed rings with a ring being at least seven-membered
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2602/00Systems containing two condensed rings
    • C07C2602/02Systems containing two condensed rings the rings having only two atoms in common
    • C07C2602/04One of the condensed rings being a six-membered aromatic ring
    • C07C2602/10One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Immunology (AREA)
  • Dermatology (AREA)
  • Rheumatology (AREA)
  • Obesity (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Pulmonology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Nutrition Science (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

WO 02/053523 WO 02153523PCT/JPOl/11083 L 7 Junlo.eiia Ceity)98 o. 1 8 1 .12 ~Jl~'ti-.Z'-A-00-U If (EA RDMA, Siene 240,b p9,98 Strct F jucnal 6, pp.cna 11-2,191Chit, 198, etl a Bioc. B1, ph182 WO 02/053523 WO 02/53523PCT/JP01111083 Res. Commun., 166, pp. 1300-1307, 1990 MiA TW-0" 44t L- 1- ~f t-h-t 0
R
2 Ar XY
R
3
R
-Z~i RI~J RI b W .CtI<(LoM:-7D±L1iIU1 WO 02/053523 WO 02/53523PCT/JP01111083 7iJ'E~i c 9 7/-At' t U cc X CN( -N 1A 4rP, 3 R ~J i C 6 7IV~~T~)\-N(RD)CON(R)- (R'RTY I Ra t) s C-XW: CI 6 7/L: (_Si2N (R9)~A 1 (R9 Th 1-~~hU ;Y 7iJ5.-OR" 1 l" ZI± Cl- 6 7iLzkA'A, Rd C 1 6 777 WO 02/053523 WO 02/53523PCT/JP01111083
R
2 TR-Y R t R R U LY R 4
C
110 cllo DCi ~i'i- 7b Lfi 7 RK R2, RU R 4 Thi~ Ar -A'7 L7CR-S Ztfl07 L) 7 1) -YR3 k;5V L~t b~4 L(K) 0i)iJ~ A r T, 7 ri7 j 1 RXN 2 WO 02/053523 WO 02/53523PCT/JP01111083 9 -~~XffiCON(Rs)a,:Vt*-lp R 5
N:
C'b; M Tt LK. 6 tJT>&7 9 L fiT- X hM-N (RD CON (R 8 R3I~C 7)A tX R' N: -LT- T 5LLMT- UXSON(9 X ff79 I'S~4 A-79 IQ$2 4-f#IM1- 79 -Mq L 9-4~~v>ThrzK.6AM'L14 57 L- J6 WO 02/053523 WO 02/53523PCT/JP01111083 Ara Ale)~ TPFh i l6h3AV 1{7W: 2 %LLQ)ODV N,7 -Y-4-f-V Zz> £1 Zz6 1)5 U L, t5 W/I M 7I ZW,--L A I -i U9 L 0D-5 P q Y LfN1 1 ~TtI t 1 L ff II AT- flyfiI R 2 *-ARA (Dr *Ng t b g WO 02/053523 PCT/IP01I11183 9 y A-I' i/kr K j t- 7 U~7 7" 1 /IMi WO 02/053523 WO 02/53523PCT/JP01111083
OH
Nio a~l OH TplO Tp22 R' Rio H H Me H Me Me iix 0
OH
x Tp3O -NHCONH- Tp4O -So 2
NH-
Tpl5O -CH 2
CH
2 TpI80 -para-Ph- Tp190 -rneta-Pb-
OH
01N( 0
OH
R
R X Tp5O tert-Bu -CONH- 'Tp6O CF 3
-CONH-
Tp 155 tert-Bu Tp170 tert-Bu -N
OH
0 1 0 N'O
N
Tpl8 y 0N Jc
H
R' R' H H H Me Me H Tp93 n Y 1 OH 1 cl 2 OH
OH
~0
N
R 4 Tp 160 H Tp175 isoPr Rl y Tp14O H OH Tpl4l H OMe Tp145 Me OH Tp146 H NHNH 2 Tp149 H H Tp200 0 Tp2lO S 17 /N OH z TP250 -CH=CH- Tp26O S WO 02/053523 WO 02/53523PCT/JP01111083 J_12 AR:4 MV) P- P 4FI{ Lz-i fli7) 7V- 7 1 tD& 1C RI M 2--CIO v A-N~ L~ U C J 43 U '9t*3 m DFA i ,101 WO 02/053523 WO 02/53523PCT/JP01111083 ttAl-ft AtIrW ql 7 1LA" MRA, A Rut rA i A Q A 4 A R t r-,l i X R q- M 0 T 6 D ff M T PPI &I f P ICI h, VI J CF, T p 0 5 0) WO 02/053523 PCT/JP01111083 OH OH OH 0 NaNO 2 IN Pt0 2 I H 2 ONO C) 9501 H 2 N I-i 1-2 OH OMe 1) NaNO 2
IH
2
SO
4 1)Tf O I 2,6-lutidine 2)A 44% H 2)MeOH/Et 3 N 34% TfO 1-3 1-4 OMe OH )n-BuLi IZnC1 2 0 NaOH 0 2) Pd(PPh 3 4 I 1-4 i31% I 52% 15 12 t 4. 54 g (37. 2 nmol) i'FI 12 il, 7 4 nl U, )JMzl, q A b 9 r 3. 72 g (53. 9 nmol) 8 ml Ut T Mr=t-t I-1 MR1I)A 5. 03 g (90 ~i~Ji- 4L-~'I-1 '11-NMR (400 MHz, DMSO-d 6 30 OC) 13.92 1 H1), 7, 70 J 12. 4 Hz, 1 7.22 J 11,7 Hz, 1 6.56 J 12.8 Hz, 2 H) 0 I-1 5. 00 g (33. 1 mmol) j/ 3 50 m 1 U Pto 2 40 m g JJ n -t A 7X U PC 2. 5 04 rml:R FZ T, i b~5 iL 7) Mt&J 5 00 m g )J n t bNigJ U, t 4L-MA4 1-2 OfLJgjt 4. 30 g (95 T) 'J 1-2 'H-NMR (400 MHz, DMSO-d 6 30 OC) 7. 10 (dd, J 10. 6, 1. 3 Hz, 2 6. 71 (dd, J 10.6, 1.3 Hz, 2 6.23 2 H) 0 'f-ilt 1-2 1. 99 g (14. 5 mmol) L* 50 ml, W%61W 22. 4 ml i"-NNY t, 0 OCi.
-C F-A 17 J-,71(M' 1. 20 g (17. 4 mmol) -7Jh 5 ml T t, Pa OD;L- VZ r fC- 3 0 3 t P 2 r' )5 IA UIt U, 7HzX-0 ;t M APJ~34i 836 nig (42 H-NMR (400 MHz, DMSO-d 6 30 0 C) 10. 24 WO 02/053523 WO 02/53523PCT/JP01111083 1 7. 15 (dt, J= 11. 7, 1. 3 Hz, 2 6. 96 (dd, J= 10. 4, 1. 5 Hz, 2
H)
0 4L-Pr*JI 1-3 420 mg 04 mmol) RU 2, 6A 9>0. 85 ml (782 mg,. 7. 30 mmol, 2. 4 A) ;L If L- 5 nil ;VP -30 0 C~7 F 9 7/1-,t1 r(TFA) 1.-8 9 g 70 nmol1) '51 ft. 3. 5 t- 7j(P U-i tt, f ppwLj 115 ml LW U, 9 c A,'7 1 ml ;L-D>C- -(Ir 41 ;0 C fW) 4 TL 4 25 8m g (3 4 tl 1 PC.Lf-L AIM I- 4 H 'l-N MR (400 MHz, DMSO-d 6 309 0 7. 45 (dd, J= 12. 9, 2. 9 Hiz, 1 7. 39 (dd, J 10. 7, 2. 9 Hz, 1 7. 10 j 12. 9 Hz, I 6. 93 j 7Hz, 111), 3. 3 H) 2 6, 7,8- F51% t 5, 5, 8,8-i xT-]~7 7 32 8 mg 23 mmo)~F L Fi27 7(THF) 3 ml t, -78 0 Cil7 -n-BuLi 1. 6 M S0. 92 ml 48 no) jjfM4-, 3 i 0 3 *L P: DMTL A ED 168 mg 23 nmol1) THF 2 ml L b L 4- fU-gL t 1 W5 $1 1-4 220 mg 82 mmol) RUPd (PPh,) 1 71 mg 062 mmol) THF 5 ml K2hjU)Jfl, Ri1LUi. 4 04m* 71 iifl*-, ffl R- T'FlU, JL-j 1-5 5138 mg (52 1 T 5: 'H-NMR (400 MHz, DMSO-d 6 7. 55 (dd, 1 HI, Pd (PPh 3 4 L 7. 47 J= 2. 2 Hz, 1 H), 7. 40 J 3 Hz, 1 7. 37 (dd, J= 10. 3, 1. 7 Hz, 111), 7. 30 (dd, J= 8. 1, 2. 0Hz, I 7. 11 J =12. 7Hz, 1 7. 07 J =10. 5 Hz, I1H), 7. 07 J =10. 5 Hz, 1 3. 87 4H1-), 1. 66 411), 1. 29 611), 1. 26 WO 02/053523 WO 02/53523PCT/JP01111083
H)~
4L-A 1I-5 130 mg 40 mmo) n2-/L- 6 ml iL 1 2 N7JZ Lt h9 A 3 m I Ut.~ 15 j 2 Nt E 4 L T pO05 3 8 m g 31 14 L-ft T p 05 FShr 161 0 C 'H-NMR (400 MHz, DMSO-d 6 30 0 C) 7. 64 J 11. 7Hz, 2 4. 78 J =2.O0Hz, 1lH), 7. 40 J 3Hz, 1 7. 30 (dd, J 3, 2. 0Hz, IH) 7. 27 J 11. 7Hz, 2 H) Anal. Cal cd for C 21 2402 C (81. 78 H 87% Found C (81.57 H)I (7.87 IN 2 :4L- TplO 6)'j)3 OH1) NaNO 2
/H
2 S0 4 OH 1)TW 2 2,6-lutidine e HN0 2) K1 71% 2) MeOH IEt 3 N 43% 1I> 1-2 11-1 11-2 N211-2 Pd 2 (dba) 3 BINAP a-:O H ODC8 2
CO
3 Me quan OH 11-3 TrPIO t/N"4 1-2 5. 38 g (39. 3 nimol) ,A E 21 ml i U, j 30 g -MAPt 0 '0:CRfl 1' 9 r7A 2. 98 g (43. 2 nimol) 15 ml DC4i3 1- 30 3Th1AL7' Uft L, E4l 9 r Ab 71. 7g (432 mmol) ~7(90 ml- nW~ t Lk-- M9STJ04K4L -C 1-r% t rAaU 3.454gg (t6. 90 g, 71 jaH4t. -t 1 11-1 'H-NMR (400 MHz, DMSO-d 6 30 9C) WO 02/053523 PCT/JP01111083 7.83 J 11.9 Hz, 2 6.81 J 11.7 Hz, 2 H) tf-'M ilI-1 300 mg 21 mmol) Xt 2. 0. 11 ml (97 mg, 1. 45 mmol, 2. 4 i A) {L/VL L, 3 ml ON U, -30 'CT 7J TFA 375 mg 33 mmol) 2 04Y -Ctt W U, -hV, -J 2 Nf.M INTJU MgS0 4 C L U~O+~ k--J 2 C-PR 4LL 11-2 135 mg (43 C-i47':. {L6 00 11-2 H-NMR (400 MHz, DMSO-d, 30 0 C) 7. 75 (dd, J 10. 3, 1. 7 Hz, 1 H), 7.63 (dd, J 1.7 Hz, 1 6.65 Jz- 12.7 Hz, 1 6.60 J Hz, 1 3.81 3 H) 0 ti8'i 11-2 310 mg 18 mmol). 2-7 6, 7, 8-5p F tt 1- V1L 5, 5, 8, 8- F f/ Iv -t 7 Vr 1-2- 240 mg 18 mmol) HlM1r z-,A 463 mg 42 mmol) 2. 5 mol Pd 2 (dba), 27. 1 mg 030 mmol)., racemic BINAP 81. 0 mg 13 mmol) 7k ~JR C, k~ -Clt M UI L, AWN ~~~~~ttkTi~L 'IMgSO, U it f -ki el E A L 7 Y t Y) L- t a s~F 3~7 f ~ii5~ L 1 it, j= 4 0 1 T, rR II-3 98 mg (19 11-zr73 'H-NMR (400 Mh-z, DMSO-d 6 30-C) 8. 51 1 7. 27 8. 5 Hz, 1 7. 15 (dd, J 13.2, 2.7 Hz, 1 7.02 J 13.0 Hz, 1 6.94 (da, J 8.5, 2.2 Hz, 1 6. 93 J 11. 5 Hz, 1 6. 55 (dd, J 11. 2, 2. 7 Hz, 1 3. 71 3 1.64 4 1.24 12 H) 0 t-LA- II-3 90 mg 27 mmol) ;k 47 HBr 5 ml i ll AL-7'U 9 Wr't WO 02/053523 PCT/JP01111083 DtcL*, APR L ll~' TplO 94 mg (quant) 'fL-2}3 TplO it, Hk A (-r37 L-A) ;iAIk, 216 'C H-NMR (400 M liz, DMSO-d, 30 0 C) 8. 58 1 7.28 J 8.3 Hz, 1 7.16 (dd, J 12.2, 2 7.03 J 11. 5 H-z, 2 7. 02 j 2. 5 Hz, 1 6. 94 (dd, J 8. 5, 2. 5 Hz, 1 H), 1.64 4 1.23 6 1.23 6 H).
IJ3 4 Tp20 XY Tp22 0-8-)t
H
2 11-2 Pd 2 (dba) 3 BINAI'>o H Br Cs 2
CO
3 50% OMe quan OH In-i Tp2O NaHCH 3 148
CH
3 CH 3 0 O HBr a OMe qa OH 111-2 Tp22 T 11-2 158 mg 60 mmol). 2-7 2-5, 6, 7, b 1L I!r2-3, 5, 5, 8, 8z -A-t:7 t7 1I/-7 131 mg 60 mmol) PeRMt zr 7 236 mg 72 mmol), 2. 5 mol Pd 2 (dba) 3 13. 8 mg 015 imiol). racemic BINAP 41. 1 mg 066 mmol) 1 7 J( t-/ZY 4 ml t 100 0 C -{Tt 4L, O 5 rf 3l Ki R DL 2-A- 4 0 1) I CI~ 4L--qqZI11-1 129 mg (50 %)ji 4-II1 'H-NMR (400 Mliz, DMSO-d 6 30 0 C) 8.14 1 7.21 1 7.11 (dd, J S13.2, 2.2 Hz, 1 7.02 1 7.01 J 13.0 Hz, I 6.91 (d, 11. 2 Hz, 1 5. 91 (dd, J 11. 2, 2. 4 Hz, 1 3. 66 3 2. 09 (s, 3 1.63 4 1.24 6 1.20 6 H).
WO 02/053523 WO 02/53523PCT/JP01111083 111-,' 1 125 mg 36 minol) t- 47 HBr 6 ml M U, Mru t" 4~h~bU MgSO 4 V~fi Utk ukr 4LA--* Tp2O C91AIfKA 131 mg (ciuan-b) MA4 mO4LtI VW L ffA5166 9C 'H-NMvR (400 MHz, DMSO-d 6 0 C) 8. 28 11H), 7. 21 1 7. 15 J 12. 2 Hz, 2 7. 04 1 6. 72 12. 2 Hz, 2 2. 09 111), 1. 63 411), 1. 25 611), 1. 30 6 H) ;Anal. Calod for C,,H 27 N0 2 1/4H 2 0 C (7 7. 2 7 H 11 N 10 Found C (77. 37 11 02 N 12 9) NaH 60 in oil 16 mg 43 nmio)n MAL_~- DMF 1 ml VN Uit 0 111~-ji l-1 100 mng 28 mniol) DMF 2 ml 1,~ i af~z tTR4Utt 0 2031k n rY r4L AA- 0. 1 ml t-J -C2 1 f A -A-40 :1-20 1) TM t, fL-A*1 111-2 70 mig (48 ?l~ft,, {L~?j111-2 H-NMR (400 MHz, DMSO-d 6 30 0 C) 7. 28 1 7. 03 1 H), 7. 01 J~11. 3 Hz, 1 6. 89 J 13. 4 Hz, 1 6. 72 (dd, J= 13. 4, 2. 9 Hz, 1 6. 22 (dd, J= 11. 3, 2. 9 Hz, 1 3. 72 31H), 3. 18 3 2. 04 3 1. 63 4 H) 1. 26 6 1. 19 6 IM -1t 111-2 65 mg 18 mmol) 47 HBr 3. 5 ml L, A L Lit 24 T'LLfA eptW Uif. 4L-A4 Tp220 f lJ-5-IA66 ing (quant) L4 L- JL -PA Tp22 J jr.V 168 0 C H-NMR (400 MHz, DMSO-d 6 30 0
C)
7. 29 7. 14 IJ 12. 4Hz, 2 7. 05 11H), 6. 65 (di, J 12. Hz, 2 3. 19 1 2. 03 3 1. 64 4 1. 26 6 1. 19 6 H) Anal. Caled for C 23 11 2
,N
1 0 2 C (78. 60 H 32 N 98 Yo) Found WO 02/053523 PCT/JP01111083 C (78.47 Ii (8.41 N (3.92 IJ4 :4L Tp30 OD OH OTs TsCl /t 3
N
H
2 N 45% HN 1-2 IV-1 COOH1)SOC1 2 1)L\N 2) NaN 3 2) Py I IV-1 OTs 87% 9 IV-2 19% IV-3 NaOO Tp3O Il=~i~ I-2 250 mg (2.07 mmol) :4Hrid-, Lz 5 ml kr U\ F' rl ~5i 4F473 mg 48 mmol), ~~rF1 7IZ~1m fai 7z J -P'f Ail*~f7L C'E±i..U Y7 MgSO' -C~rr~l L, tt-'t j I-1 245 mg (46 j 'H-NMR (400MHz, DMSO-d 6 7.77 J 8.3 Hz, 2 7.41 J 8.5 Hz, 2 7.22 2 H), 7. 05 J 11. 2 Hz, I 6. 98 J 13.2 Hz, I 6.96 (dd, J 13.4, 1.7 Hz, 1 5.92 (dd, J 11.2, 2.0 Hz, 1 2.40 3 H) 0 6, 7, trl~ 51 5, 8, 8-5 9 11 7 3rL 27 /iR; iE 500 mg 16 mmol) Zz1 5 ml, it- 2. 56 g 1,710, X L, j sUi LO" 2 RUrpif A, VA J71 F- 5Uni l L, 7 4l t f 9 r 7 238 mg 66 mmol) 7J( 1. 2 ml G U-fiCV -C 35'-40 0 CI 30 351R4 Lk'. ZJ~JI WO 02/053523 WO 02/53523PCT/JP01111083 {L~IV-2 :'H-NMR (400 MHz, DMSO-d, 30 0 C) 7. 89 J 2. 0 Hz, 1 7. 68 (dd, J8. 3, 2. 0 Hz, 1 7. 51 if8. 3 Hz, 1 1. 66 4 1. 25 12 H) 0 f L-6'10z TV-2 206 mg 80 mmol) 3m1 &6 L, 3ii~bLIt. 2 PirpliI, R U, 4LI-K- IV-1 200 mg 69 mmol)*2/7'T /O9 (DMAP) 8.9 mg(0. 072 mol) %5NU2~t 20 Wff' P!:U 7J<.LJl.
-CU, WU, T>F LIA L24' U, 7MfUL~ A Ahc-c--&h "Jr1 MgSO 4 TIO I, C-Ait IV-3 68 mg (19 J-t JLm IV-3 :'H-NMR (400 MHz, DMSO-d 6 9. 27 1 8. 81 I 7. 80 J 1 Hz, 2 7. 50 (dd, if 11. 7, 1. 9 Hz, 1 7. 45 j 8. 5 Hz, 2 7. 38 J 1. 9 Hz, 1 H), 7. 37 (dd, if= 16. 8, 2. 5 Hz, 1 7. 34 J =11. 2 Hz, 1 7. 23 Ji= 12. 6 Hz, 1 7. 16 (dd, J= 8. 3, 1. 9 Hz, 1 7. 14 Jf 13. 2 Hz, 1 H), 2. 42 H1), 1. 62 3 1. 22 6 1. 21 6 H) 0 ILV- 13 60 mg 12 mmol) 7Jf4tbJ7A 40 mg 12 ml 71J YI L L ~hU, A -V IUft.
0 6 NNi 60 OC 9 7j(, EET W U-C %2 N:W&C'PH 5-5.0 ZU NIj<,,A fVT*?"7J(TCAV '1 MgSO 4 V U1%t7-A L 7:7 'y 'YV' r Y' 4 z A- U, 4L-to
T
p 3 O 25 mg (59 t 4fL-W^-t Tp3O 0/s ~L 207 'C 1 H-NMR (400 MHz, DMSOd6, 30'C) 8. 78 1 8. 59 1 7. 57 J =12. 2Hz, 21H), 7. 37 (d, Ji- 2. 2 Hz, 1 7. 22 if= 12. 2 Hiz, 2 H1), 7. 20 if= 8. 6 Hz, 1 7. (dd, Jif 2. 2, 8. 6 Hz, 1 1. 62 4 1. 22 6 1. 21 6 H) Anal. Calcd f or C 2 2 11 2 6 N_0 3 1/2H 2 0 C (70. 38 H 25 N 46 Found C WO 02/053523 PCT/JP01111083 (70.32 H (7.21 N (7.37 Vq 5 :4L8-tTp40 OH OMs MsC /Et 3
N
H
2 N 45%H 2
N
1-2 V-1 OMs om CtS03H SOcl pyridine! V-1 o., 98% 12% V-Z V-3 NaOH quant 0, O Tp4O 1-2 1. 00 g 30 mm1) 2AI4 J 1- 10 ml t L. F F A7 1. 5 ml, Zi Pl2 -f 1-836 mg 56 ml, 7. 30 mmol) ONarT, 1L U ft.L~z 2 8 F rpl ig A 'R 7 y 9 Y; 7FJ t 13; J, 3 7 4 4L--t V-1 828 mg (52 IiP. L V-1 'H-NMR (400 MHz, DMSO-d 6 3000) 7. 29 (bs, 2 7.24 (dd, J 12. 2, 1. 0 Hz, 1 7. 13 J 13. 2 Hz, 1 7. 02 (dd, J 13. 2, 2. 0 Hz, 1 6. 02 (dd, J 11.7, 2.0 Hz, 1 3.33 3 H) 0 3 tlA;L-7 A- 2. 0 ml 0 OCIC 1, 2, 3, F H 1- V 1, 1, 4, 4-7i 7( ~A-'t7 Yr 1. 00 g (5.32 mmol) I)J-~x tJ 1 kk7j(,1.
V-2 ~$hItY 1. 50 g VI~i~ {-1i V-2 'H-NMR (400 MHz, CDCL 3 7. 93 J 2. 2 Hz, 1 7. 74 (dd, J 8. 6, 2. 2 Hz, 1 7. 52 J 8.6 WO 02/053523 WO 02/53523PCT/JP01111083 Hz, 1 11), 1. 73 4 1. 33 6 HI), 1. 32 6 tLp'L140 V-I 200 mg 93 mio1) 4L',j-IW V-2 267 mg 93 inmol) -PIIzJ. tf1)~ -3ml iLAAU rETA ~i Uk 0 2 *Ir1l~k 7JQJ-fZ. 7 -q SL N WR WP-fi*-% MgS 4 %%Uk ,AM Uft. Y i A Yr, 7 7-f- (WFR-XV) -0OH 1- L-M'"V-360 mg (12% {L-4PC .tt; V-3 'H-NMR (400 MHz, DMSO-d 6 30 0 C) 10. 94 1 7. 73 (s, I1H), 7. 58 2 11), 7. 51 J =10. 7 1z, 1 i1), 7. 30 (dd, J =13. 5, 2. 7Hz, I 7. 21 J= 13. 2Hz, il-1), 6. 89 (dd, J= 10. 9, 2. 7Hz, 1 3. 42(, 3 1. 63 4 1. 22 6 1. 20 6 HL~ 4L-V'i V-3 45 ing 097 imo) Y2--37,'-'I3 ml, 2 N7J3' fb~ t 1 ml U~h k U7 6 VTrliJ! 2 N AM-- t L L 4 t SMgSO 4 ,C*,1P-A SA~tf. tmL Tp40 -)fI~Ut 6 211 9C 'H-NMR (400 MHz, DMSO-d., 3000) 10. 11 1 7. 53 (d, J 2 Hz, 1 7.561 J 3 Hz, 1 7. 44 (dd, J 3, 2. 0 Hz, 1 7. 13 J= 12. 2 Hz, 2 7. 19 J= 12. 5 Hz, 2 1. 61 411), 1. 21 6 1. 13 6 H) Anal. Calcd for C,,H 2 BNlO 4 Sl C (65. 09 H1 50 N 61 Found C (64. 84 H 47 N 69 16 C4~Tp50 O-A- 0 0 R0
OH
R COCd DMAPI-I R 0 0 0aH RQ N0 IN
H-
H 0) 0pyridine
RR
VI-1 (R =tert-Bu) VI-Z (R =tert-Bu), 92% Tp5O (R tert-Bu), 42% VI-3 (R CF 3 V1-4 (R CF 3 80%/ Tp6O (R CF 3 5 3%O WO 02/053523 WO 02/53523PCT/JP01111083 3, APf 550 mg 00 mniol) bl MOIUtc-' 1- WI? V VT-i :L-81t 1-2 158 mig 15 mmol)~ 10 ml, DMAP 1 )t 9T4 zk A- N JM 4 U 2 1) -Ct&L 4E7 -410VI-2 600 mg 4LIV-2 600 mg 05 mo:1- r -'10 ml -c'5 A 4LAF 2.10 ml fl -Lti j2 Nt 30 ml i- PH 2 L O T U A FtW4 9p Lft 0DS7, F 74 ,L -v (th9 A- 2 1 J -rr, L, 4L- 1IV TpSO 149 mig (42 K4JTp5O 2 9 f2A (lA4L' 236 0 C;Anal. Calcd for C 22 H,,N,0 3 C (74. 76%/) 1(7.70 N(3. 96 Found C(74. 56 H(7. 63 N(3. 82 INJ7 :4 3,5-1 :7 9 7 I 1KfL V VI-3) 560 mg 02 nimol) 4l VA 1-2 137 mig 00 mmo)~ If 9 $-z5 ml, DMAP 1 it -hfl X -Al 2 1) -C UX4Lg VI-4 500 mg (80o1/) L-~~iVT-4 H-NMR (400 MHz, CDCT 3 9. 00 1 8. 47 2 11), 8. 39 21H), 8. 12 11H), 8. 03 11H), 7. 70 j =12. 1Hz, 21H), 7. J 12. 1 Hz, 2 H) {L~VI4 500 mg 81 imo) =5 7/ -AL6 ml 4)F9 ~Y~3 ml li1~i t- 7" L z.S 4rA-' 2 N 3 0 mi WO 02/053523 WO 02/53523PCT/JP01111083 PH 2 L 51 -UF 9 t,, L Tp6O 160 mng (53 f {L'AI Tp6O X j7C, RwVA149-150 0 C 'H-NMR (400,MHz, CDCl 3 8. 33 2 8. 09 1 8. 05 I1 7. 71 J= 11. 3 Hz, 2 7. 38 J =11. 5 Hz, 2 H) Anal. Calcd f or C 16
HN
1 0 3
F
8 C (50. 94 H 40 71 Found C 87 H 70 N 44 0118 4L121 Oj Tr)8 0, Tp 8 2 Y T p 8 4 1- A 0 CO1)SOCI 2 N iili1 1)4 H 0 Oa2) pyrine( DMAP 11-2 -0 82%
VIM-
O 0 1) NaOH 0 N aH0 O 2) Ac 2 O/pyridirie w H I W H 9%VU-2 Tp8O 1) NaHl 2) CH 3 I, 660k O 0 0 fAc 0 H N!O N w~ I wI VIU-3 Tp82 6, 7, 8 Vh1r5,,8, h 92vfrAt7 2 /'rX7 00 g 2 mmol) A A-18. 0 g, 20 ml P-MU 1 1AR9MI UP-, 2 *-pjMWiMt 5-7 17ThZ2. 07 g (15. 1 nniol) t-V It, 41 7 J(h' 9 $f-9 20 ml iIL DMIAP 100 0 C-CRO Uft 1 UV, C#MU 2 N AR MfPth -C N MgSO 4 WO 02/053523 WO 02/53523PCT/JP01111083 44Wz~zz 1 -2 0) Tri UL-Pt1 VII-1 6. 96 g (82 %~t 0
'L
i~VII-1: 'H-NMR (400 MHz, CDC1 3 8. 13 J 2. 0 Hz, 1 7. 98 1 H), 7. 90 (dd, J 8. 3, 2. 0 H-z, 1 H1), 7. 86 J= 2. 2 Hz, 1 7. 56 (dd, J= 8. 3, 2. 0 Hz, 1 7. 41 J= 8. 3 Hz, 1 7. 40 1 7. 38 J= 8. 3Hz, I1H), 7. 29 (bd, J11.7 Hz, 21H), 7. 29 I1H), 1. 72 8 1. 33 6 1. 32 6 1. 31 6 1. 29 6 H) 0 ML-'I~g VII-1 6. 96 g (12. 3 mmo) ml, z-W-A,40 ml i,.
_4 L, 2 N &1 4K hJ 57 A 3 0 ml lk)Jn RTR P 2 0 rp 2 N :tR fR'iL Uf, ;Ah'S I O U t-W ji~~ MgSj i1--t t 7. 35 g (quant. 6D*1-" 6. 43 g ,u 7J(.e 9 2 '0m 41 Ill- i3 0 m1 I 'L7 7 tJ 2 F1{ 4 m k, A/ 4A~zz 1 3 -LC--rj t 'fL tA- VII-2 4.12 g (95 Y) O tE-N't VII-2: 'H-NMR (406 MHz, CDCl 3 7. 87 (br s, 1 7. 84 J= 2. 0 Hz, 1 7. 54 (dd, J 8. 3, 2. 0 Hz, 1 7. 53 2 7. 43 j 3 Hz, 1 7. 23 J12. 0 Hz, 2 2. 34 3 1H), 1. 72 4 1. 34 6 H) 1. 31 H) 0 t-ISA'A VII-2 4. 12 g (10. 5 mmnol) 9t-L V zZ- 50 ml,-r3 40 ml 74 1 U, 2 N~jT~ hf''tt 9 40 mil T3D-Wl 0 n 2 Oji1j 2 N J t, ft% f U -C Tp 80OD R- ZV 2. 9 0 g (9 1 ;LIi t Tp 8O0:t" j YplY A 3t 1 rRIVA 209 0 C 1 INMR (400 MHz, CDC1 3 7. 83 J= 2. 0 Hz, 1 7. 73 1 7. 71 zJ 12. 3 Hz, 2 7. 54 (dd, J 8 2 Hz, 1. 8 WO 02/053523 WO 02/53523PCT/JP01111083 Hz, 111), 7. 42 J 3 Hz, 1i 7. 36 j =12. 1lHz, 2 1. 72 (s, 411), 1. 33 6 1. 31 6 H) Anal. Calcd for 222,,N3 C (7 5. 19 H 17 N 99 Found C (75. 24 11 27 Yo) N 90 NaH (60 31 mg, 0. 76 mmol) 1i\CV DMF 1 ml LUiUf, ~~f-~IJVII-2 200 mg 51 mmol) -ar DMF 3 ml L) 7Ct, MC- 1, t. 5f& E r ~4L 1-/1J0. 1 ml ;EN% Lft 30$~ 3 7J t I-'~97 1 I) -Cr- JUC 4Ej-;t1K VII-3 136 mg (66 ;Ifl {Ko S1V VII-3: '11-NMR (400 M H-z, DMSO-d 6 300C) 7. 32 J= 8. 1 Hz, 1 7. 26 (dd, J= 8. 1, 1. 7 H1z, 1 H1), 7. 16 J= 12. 2 Hz, 2 7. 13 J= 1. 7 Hz, 1 H) 7. 10 J= 11. 7Hz, 211) 3. 35 31H) 1. 55 4 H) 1. 18 611) 1. 01 6 E)~ 'L VII-3 133 mg 33 mmol) ~zu 8 ml U, 2 N *M4'L JiW~~bU/O ~ni(CM "MgSO 4 V+I~L U7r. 'f Uc.
Tp82 MR t RM 120 mg (quant.)Itc Tp82 L 2 94 C 'H-NM4R (400 M Hz, DMSO-d 6 30 0 C) 7.28 J 8. 0 Hz, 1 7. 27 12. 0 Hz, 1 7. 20 (dd, J= 9. 0, 1. 7 Hiz, 1 11), 7. 07 J 7 Hz, 1 7. 01 J- 12. 0 Hz, 2 HI), 3. 32 3 1. 53 4 11), 1. 16 6 0. 97 6 H1) Anal:' Caled for C 23
H
27
N
1 0 3 1/41-120 C (74. 67 H 49%Y) N 78 Found C (74. 91 H 58 N 71%) 6,7, 8- b F 5, 5, 8, 3- -F V-7 -;Z -C TOSO L U -C Tp84 U L, Tp84: (L WO 02/053523 WO 02/53523PCT/JP01111083 z) AR 206 0 C 'H-NMR (400 MHz, CDCl 3 7.72 J= 12. 0 Hz, 2 HI), 7. 45 (bs, 1 7. 41 1 7. 37 J 12. 0 Hz, 2 7. 1 2. 46 3 1. 70 4 1. 30 6 1. 29 6 H) Anal.
Calcd for C 23
H
27 N0 3 C (75. 59 H 45 N 83 Found C (75. 49 H 50 N 64 06 9 tL-tTp88 016' 0) t{L A-45t ',Tp8 8 4L-. Tp8 8: ~I'~142 cC 2 11-NMR (400 MHz, DMSO-d 6 30 O(D) 10. 16 1 HI), 7. 83 (dd, J=8. 6, 2. 2 Hz, 1 7. 73 J= 2. 4 Hz, 1 7. 72 J 12. 2 Hz, 1 7. 22 J 12. 2 Hz, 2 7. 08 J 8. 8Hz, 1 3. 88 3 H), 2. 0 7 6 H) 2. 0 5 3 1. 74 6 H) Anal1. CalIecd f or C 25 H1 2 7N 1 0 4
H
2 0 C (70. 90 H 90 N 31 Found C (71. 19 H 94 Yo) N 31 04 107 Tpi 6 D/V\4L TpO {Kt~Tp9O J( (J 149 0 C 'H1-N\MR (400 MHZ, DMSO-d 6 30 10. 23 1 H1), 7. 82 J 12. 2Hz, 2 7. 56 J= 15. 6 Hiz, 1 7. 56 1 7. 34-7. 42 (in, 2 7. 25 J= 12. 2 Hz, 1 6. J15. 9 Hz, 1 3. 65 4 1. 27 6 H1), 1. 25 6 H) Anal.
Calod for C 24
H
27
N
1 0 3 -1/4H 2 0 C (75. 46 H 25 N 67 Found C (75. 47 H 31 N 59 Yo).
WO 02/053523 PCT/JP01111083 Cl SCOH 1)SOC1 2 N 2) pyridinef DMAP I TV-i H 9.2% Tp93 6, 7, 8- F t fl-5, 56,8, 8-5 VI -A -A'±73 L- 2-f 77 91 11-R 355 mg 45 mmIol) 1,l~krh~-IV 1. 73 g, f 5 mI LDJJ L, M it UfL 2 Wfilfk, UL 'j IV-i 400mg 45 mmol) j 7 9j l 5 ml i5m tL- DMAP 53 ing 44 immol) JJP 100 'C -C"Itit Lt JA, 7ffl ut-iil-U 2 N MgSO T' Uk L IC Ah i~f L, Pt. 9 YA- t Y b, rl -7 3 Y 7 i' 7 (ffrki zlt A- Zz 1) TOW UN RItTp93 48 mg -kil~fc 4L' it Tp93 17 9 ZC.A Fi- iI 241 9C 'H-NMR (400 MHz, DMSO-d 6 10.05 1 7.99 J 11.0 Hz, 1 7.91 (dd, j 11.0, 2.2 Hz, 1 7.60 J 16.1 Hz, 1 H4), 7.58 J= 2.2 I-z, 1 7.55 (dd, J 13, 2, 2. 2 Hz, I 7. 36-7. 42 2 7. 24 J 13. 2 Hz, 1 6. 78 J 15.7 Hz, 1 1.65 4 1.27 6 1D, 1.24 6 04J 12 4UP9it Tp95 OD -083Z E) 6, 7, 8-5 t i 5, 8, 8- F7 3r 1, -2--f 3 li 4 -W PP U-C I 6 tV4 t L Ut. 4 t Th Tp95 'A%97 9 XA 216 'C; 'H-NMR (400 MHz, CDC1) 7. 71 J 11. 9 Hz, 2 7. 53 (dd, J 10. 8 Hz, 14.9 Hz, 1 7.29-7.37 5 7.18 (brs, 1 6.95 J 15.2 Hz, 1 6. 85 (dd, J 10. 8 Hz, 15. 4 Hz, 1 6. 04 j 14. 7 Hz, 1 1. 4 1.31 6 1.29 6 H) 0 WO 02/053523 WO 02/53523PCT/JP01111083 Od13 :4L-'-it Tp140,. Tpl4l R jY Tp145 6D8- By r 'mS- -/Pd(PPh 3 2
C
2 I j Et 3 N Cul 79 Ts
K
2 C0 3 0 94% V111I.1 VITI-2 Pd(PPh 3 2 C1 2 I CuIi /Et 3
N
11-2 81% 4141l
NH
2
NH
2 1 NaOH qtiant
TH
2 6.6% Tp14O Tpl46 Tpl49 OMe Tll Pd/C/H 2 I 0 NaOH 86% VIII-3 Tp150 2- i/ 12-- 5, 6, 7, b 11-5, 5,8, 8-t~ b I77y 3. 00 g (11. 2mmol)R-OQ, 1"fLMR237 mg l2nimol) T.z$T 225 ml ~Ch~~c~~TO -7-t zH- 3. 31 g (33. 7 inmo) /tr Pd (PPh)C1 786 m g(1. 12 mmo 1) 0 /4 7 0 'C 1 UIcO 2 2flT& P49~U f-.4 1 OR t t NH 0OH/ NH 4 C 9/ 1 7(X I 7R. N -W 4L--01 VIII-1 2. 51 g (79 4LjRj- VII-I 'H--NMR (400 MHz, CDCL 3 7. 40 1 HI), 7. 21 2 1. 66 4 1. 26 WO 02/053523 WO 02/53523PCT/JP01111083 6 1. 25 6 0. 24 9 H) 0 J'fK t VILE-i 1. 00 g 52 mmol) 31 15 ml L 9 Ah 97 mg 70 mmolI) 2VAT. i' 24 PRPMIR4O L7Jt ii*-f7'., 'f~tiVIII-2 700 mng (94 -6 -#AJ VIII-2: 'H-NMR (400 MHz, CDCL 3 7. 44 1 HI), 7. 26 2 3. 01 4 1.27 6 1. 26 H), 4tJ'jVII-2 136 mg 64 mmol)RV~fL-t 11-2 160 mg 61 mmol) kF 3 J5/7~J 6. 0 ml Ll Ti JI: XAL, ci Pd (PPhl) 2 C1 2 112 mg 16 mmol)BzRJM El L1I 30. 5 mg 16 nimol) )JIII%.
I1) ICMi Tpl4l 171 mg (81 t-4L TP141 (1WL /J 1- 94,A 139 OC; 1 H-MR (400 MHz, DMSO-d., 30 0 C) 7. J1. 7 Hz, 1 7. 41-7. 46 (in, 2 7. 37 J8. 1 Hz, 1 7. 28 (dd, J= 8. 1, 2. 0 Hz, 1 7. 02 j 13. 0 Hz, 1 6. 97 J 11. 0 Hz, 1 3. 89 3 1. 65 4 1. 26 6 1. 25 6 H) ;Anal.
Calcd for C, 4
H
26 01 C (83. 20 H 56 Found C (82. 93 H 63 {L-JA Tpl4l 125 mg 36 nimol) 8 ml, 2 N *JRb tt 3 4m 7) II* It 3 R 2 N 'L It i ,M 9-L- M fJV\MgSO 4 TitUA I-t-k fLAltTp140 ~123 mg (quant) t-ff0 4-8910iTp1 40 j4k*Xp~- O~li 182 'C 'H-NMR (400 MHz, DMSO-d 6 30 0 C) 7. 53 J 11, 7 Hz, 2 7. 43 Jz- 1. 7 WO 02/053523 WO 02/53523PCT/JP01111083 Hz, 1 7. 36 J= 8. 1 Hz, 1 7. 26 (dcl, J 8 1, 1. 8 Hz, 1 7. 09 (di, J= 11. 7 Hz, 2 1. 64 41H), 1, 25 611), 1. 24 6 H) Anal.
Calod for C,,H1 4 01 C (83. 10 H 28 Found C (82. 83 H 42 4L L7(, T1p140 L[FIQP UMtKirTDl45 Rf-iV{L14T15:~ 791 go2 (JWL/ JI-' V :k JAA 137 "C 'H-NMR (400MHz, CDC1 3 7.62 (ci, J =12. 0 H1z, 2 7. 42 1 H1), 7. 30 J 12. 0 11z, 2 11), 7. 16 (s, 1 11), 2. 43 3 1. 68 (4 411), 1. 284 6 1. 278 6 Anal.
Caici for 024112602 C (83. 20 56 %)Found C (82. 92 H 73 'f14 JL it Tp 146 X'z Y Tp 149 Th) 4L-I1[ 9Tp141 332 mg 96 nimol). A2-)1/ 2 ml, 2 ml, 80 %L I-- /*TJI 2 ml OAA R6- 10 3 U/MOM U CtIp U 0l1)RIt' 299 mig (90 4:'ij 4Ltt I Tp146 :'H-NMR (400 MHz, DMSO-d., 30 0
C)
9. 19 11H), 7. 48 (dd, J =11. 5, 1. 7Hz, 1 7.41 (ci, J 7z, 1 H), 7. 36 (dcl, J=12. 2, 1. 7 Hz, 1 7. 32 (di, J 8. 3Hz, 1 7. 21 (cid, J 8. 0, 1. 7 Hz, 1 6. 99 J=11. 2 Hz, 1 6. 74 (di, 'j 12. 0Hz, 1 H), 00 (bs, 2 1. 64 4 1H), 1. 25 6 H4), 1. 23 6 H) tl- 1t Tp146 250 mg 72 nimol) :O 1 ml, 7J 4 ml i-,,AU Mfil~ )A L 04 L, 'L 2N t -flti7 1~\MgSO 1 4 WV ULtc A t V 7 b 2 A' 1 0 0 1) I U, Tp149 15 mng 6 {-4jTp 149: 'H-NMR (40 0 MHz, CDCL,) 7. 45 (di, 1. 7 Hz, 1 WO 02/053523 WO 02/53523PCT/JP01111083 11), 7. 30 J= 10. 7 Hz, 1 7. 28 J= 10. 3 Hz, 1 7. 22-7. 26 (mn, 2 7. 08 (dd, J= 12. 0, 8. 5Hz, 1 6. 97-7. 003 (mn, 2 1. 57 411), 1. 30 1. 28 6 H) 0 TP141 80 mig 23 mno) m-Y -IL,5 ml U, Pd /C 20 mg -tU%.Z C- Vh he, R L PC 2 q-RJA,1 4ii T 1~ rA M9 4 A 4' 2 :1I) -C-NJt 4L-ji-tVTII-3 35 mg (43 %o);L,4f/t -1VIII-3 :'H-NMR (400 MHz, CDCL,) 7. 23 J 3Hz, 1 7. 22 (di, J 11. 0 Hz, 1 7. 14 (dci, J =12. 4, 2. 0 Hz, 1 7. 00 J 2. 0 Hz, 1 6. 94 (di, J 8. 1, 2. 0 Hz, 1 6. 85 J= 10. 2 Hz, 1 6. 64 J 10. 5 Hz, I 3. 92 2. 83 4 1. 66 4 1. 27 6 1. 22 6 H) 0 4KIm VIII1-3 34 mng 097 inmol) 2 ml U, 2 N *Nj'4Lt 7 9 I I 1 m R aJ{ ?R-C't 4t Lft 12 V, RI 70 0 G 6 OTWUiP-UO 2 N ~r i -'~hU MgSO 4 "r TPl50O D~h 28 mng (86%)i1O 4L-'t1* Tpl5O (rI -A ij~i,~ 138 9C ;'H-NMR (400 MHz, DMSO-d., 30 0 C) 7. 29 J11. 5 Hz, 2 11), 7. 19 (di, J8. 3 Hz, 1 7. 12 (di, J =11. 7 Hz, 2 7. 05 J =2.O0Hz, I1H), 6. 96 (dci, j 3, 2. 0Hz, I 2. 70-2. 85 (mn, 4 1. 60 41-H), 1. 20 6 1. 17 6 H) Anal.
Calcd for C 23
H
28 0 2 .1/4H120 C (81. 02 1H 42 Found C (80. 85 Yo) H 28 i16 TLPi T15 5 OD#II WO 02/053523 WO 02/53523PCT/IP01I11183 204 0 C 1 11-NMR (400 MHz, DMSO-d 6 30 0 C) 7. 60 J= 11. 7 Hz, 2 H7), 7. J 7Hz, 1fH) 7. 36 J 7 Hz, 2ff) 7. 16 J =12. 0Hz, 2 H) 1. 29 18 H) Anal. Calod for C 23
H
26 01 C (82. 60 H 84 Found C (82. 46 H 93 o 'fJ 17 4'9JTp160 O'j-)R
OH
NH
2 1) H 2 S0 4 NaNO 2 1~ N 2) NaGH tropolone 23% P0 2-7 T -5y,6,7, 8- F 1h-5, 5, 8, 8-:7 ;g 77 -97 10 2 mg 50 mmol) i 30 7)L1Y 2 ml W U L 7 '6 T Lt,, 7 70 ing, 712 ml 1 3f .L -C+PL-iUPt t 0) 10 %7A(RP% u/2 mnl *r-z 270 mg 57 mniol) kr-lUfrjf ;ft T- Z tZ Ar2P;-' -~Lt t OD S 7 F Y- t i-7 4 Y 7- P L-/WL 2? A 185 00 'H-NMR (400 MHz, CDOD) 8. 21 (dd, J 1. 6 Hz, 10. 7 Hz, 2 7. 90 J 0 Hz, 1 7. 65 (dd, 2. 0 Hz, 8. 4 Hz, 1 7. 49 (dd, J 1. 3 Hz, 10. 5 Hz, 2 7. 45 (d,J 8. 4 Hz, 1 1. 74 4 1. 37 6 1. 33 6 H) 0 {18 K T p 170 ODR' Tp17 0 j~r5ZU ft. 4 Lt'i Tpl17O0 iR1L-tkAJ RAt 199'-201 00 'H-NMR (400 MHz, DMSO-ds, 30 0 C) 8. 12 J =12. 0 Hz, 2 7. 71 J- 1. 7 WO 02/053523 WO 02/53523PCT/JP01111083 Hz, 2 7. 61 J= 1. 7 Hz, 1 7. 36 J 11. 7 Hz, 2 1. 35 (s, 18 H) ;Anal. Calcd for C 21 H,6NO, C (74. 53 H 74 N 28 Found C (74.38 H (7.80 N (8.19%) 3, f 9 4-4 -f >7O 0 y IfL r, I-, -C fY1 17 OD)& 4ft 'fL8Tp 175 jtLft 0 U c 4L/KTp 17 9 -A-'17k) Fj',A 5145 0 C 'H-NMR (400 MHz, DMSO-d 6 3000) 7. 91 J= 12. 7 Hz, 1 7. 88 1 7. 50-7. 55 (mn, 2 7. 35 1 7. 19 J= 12. 7 Hz, 1 4. 32 J= 6. 8 I-Jz, 1 HI), 1. 69 4 1. 32 6 1. 29 (s, 3 1. 28 6 HI), 1. 28 3 H) ;Anal. Calcd for C 2
,H
3
,N
2 0 2 C (76. 16 H 99 N 40 Found C (75. 88 H 96 N 44 t-l-t Tp180 6D-M Br I AIC 3 1) n-IuLi ZnC1 2 2) Pd(PPh 3 4 1-4 X-1 (para), 99% X-3 (meta), 78% OMe OH -NaOH :-o X-2 (para), 29% Tpl8O (para), 24% X-4 (meta), 43% Tp19O (meta), quant 2.0O0 g 58 mnol1) V 4L~1>10 ml I T 4 A 6 3 mg r Jft -0 7 P 4J7(4I R 1t,,9-,af ',W WO 02/053523 WO 02/53523PCT/JP01111083 lz '2A N J'~Y fl~~i\MgSO 4 (400 MHz, CDCL,) 7. 53 J 6 Hz, 2 7. 47 (di, J= 2. 0 Hz, 1 7. 43 J 6 Hz, 2 7. 37 J 3 Hz, 1 7. 31 (dcl, J= 8. 3, 2. 2 Hz, 1 1. 72 4 1. 33 6 1. 31 6 H) Anal. Calcd for C 21
H
24
N,
2 1/41,O C (73. 98 H 24 N 22 Foundi C (74. 11 H 27 N 28%) 4L-HI*j X-1 275 mg 80 mmol) t- TU1F 3 ml ~78 O n-BuLi 1. 6 M z 0 .60 ml 96 innol1) -Vt 30 ftE U1~ rt. -0 1LCn 109 mig 80 mniol1) t- THF 2 ml i~ ,L L V, 7 2V ft. 1 H; m 1%z fL t-f 1-4 152 mg 54 molX)kRUPd (PPh 3 4 46 mng 040 inmol) t- THF 4 ml ,f 6D~ O JI)a iI L, tt 4. 5 7jZNfl x 2 1Rgt: -L 07 2 -CfmU, f E'tX-2 91 mng (29 1M~ X-2 'H-NMR (400 MHz, CDCL 8 7. 66 (di, J 8. 3 Hz, 2 7. 60 (dci, J 12. 7, 2. 0 Hz, 1 7. 52-7. 56 (mn, 3 7. 33-7. 41 (mn, 3 7. 36 (cid, J3 12. 4, 2. 0 H-z, 1 6. 88 (di, J =10. 5 Hz, 1 4. 01 (s, 3 1. 74 4 1. 36 6 1. 33 6 H) 0 IE84X-2 85 mig 21 in o1) 8 ml 2 N 71 Nft I 9 I 7 J>.3 mlIf T 4 U t 6 H rjlf 2 N Mt-i- 0M-j- ~Ajl Tp180 20 mig (24 4Li-!Kz Tpl8O ~4~iik j ,212 9C 'Th-NMR (400 Mlz, DMSO-d,, 0 CD) 7. 73 (di, J= 8. 3 Hz, 2 7. 71 (di, J= 10. 8 Hz, 211), 7. 65 (di, J WO 02/053523 WO 02/53523PCT/JP01111083 8. 3 Hz, 2 7. 59 J= 1. 6 Hz, 1 7. 45 (dd, J= 8. 3, 1. 6 Hz, 1 HI), 7. 40 (dd, J 8. 0 Hz, 1 1. 67 4 1. 31 6 1. 27 6 H).
{~J21: JL- Tpl9O 01-d) 3- T ASF-W W$q U -CjI 20 OtVA L Tp 190 ;L M" A UPL.C A~ TP190O: (It*5k 140 9C 1
H-NMR
(400 MHz, DMSO-d 6 300C) 7. 75 J =12. 0 Hz, 2 7. 75 (bs, I 7. 63 (dt, J 4. 4, 7. 3 Hlz, ,I 7. 60 J 2. 0 Hz, 1 7. 53 J 4. 9 Hz, 2 7. 45 (dd, J= 8. 3, 2. 0 Hz, 1 11), 7. 40 J 8. 3 H1z, 1 7. 30 (d, J11. 8 Hz, 2 1. 67 4 1. 31 6 1. 27 6 {22 :4-1JTp200 OD-d SBr -~Pd(PPh,) 4 1) X in-BuLi /ZnC 2 +o (HO) 2 B X Na 2
CO
3 o 2) Pd(PPh 3 4 1 1-4 XI-1 (X X1-3 (X 42% X NaOH A X1-2 (X 19 Tp200 (X 155% XI-4 (X 4801 Tp2lO (X 2- 5 t 1 5, 5,8, 't tfi4 7~ -'57 V 3. 00 g (11. 2 imol) /'zXJ Pd (PPh 3 4 416 mg 36 mmo) =fT 2/ bz w 3. 6 ml t, 10 31M1MOL, Pt, 2--7 -ZJ '4Y 1. 45 g (12. 9 mmol) tbI1 1- iM~ 9rYb.6 M2 8 ml I bR1ijR n 5. 5 04l1-.k, 7 ~~rt\MgSO 4 UA Ltif{l riALT'f UfA b~7-f v~1:50)~4L~I-11.00 WO 02/053523 WO 02/53523PCT/JP01111083 g (35 t-14ki XI-1: 'H-NMR (400 MHz, CDCL 3 7. 61 J= 2. 0 Hz, 1 7. 44 J= 1. 1 Hz, 1 7. 42 (dd, J= 8. 1, 2. 0 Hz, 1 HI), 7. 31 J 3 Hz, 1 6. 58 J 3. 4 Hz, 1 6. 44 (dd, J 3. 1, 1. 1 Hz, 1 H), 1. 70 4 1. 33 6 1.,29 6 {LI~-1 497 mg 96 mmo1) t-THF 4 ml U, -78 'C C't- n-BuLi 1. 6 M 1. 84 ml 94 mmol) Jfl 30 3 4RYR 1 Y. L 4 J4LP- M 267 mg (1.96 mmo1)-t TJHF4 ml 1 WPM, C.tL{L 1-4 370 mng 30 mmo1) RflYPd 4 75 mg 065 mmol) -qS 1 4 2 N~ Jgk l AVPCAlA\ MgS0 4
LM
W 4L-A4,j XI-2 142 mg (19 Yo) Az4t 4L ^A 4 XI-2 1 H-NMR (400 MHz, DMSO-d 6 309C) 7. 81 (dld. J= 12. 7, 2. 0 Hz, 1 7. 71 J 1. 7 Hz, 1 7. 69 (dd, J 10. 3, 1. 7 Hz, 1 7. 54 (dd, J 1. 9 Hz, 1 7. 39 T 8. 3 Hz, 1 7. 15 J- 3. 7 Hz, 1H), 7. 12 J= 10. 5 Hz, 1 7. 09 J 12. 9 Hz, 1 7. 07 J3. 7 Hz, 1 3. 89 3 1. 66 4 H), 1. 31 6 1. 26 6 H) 0 t-!N'4 *XI-2 135 mg 35 mmo) =37 4 ml 2 N AKO th 1] 4UZ 1. 5 ml -Mk t!1f M.-l t 2 Pj. RIM V dU 2 N71 MHz, DMSO-d, 30-C) 7. 91 J= 12. 0 Hz, 2 H1), 7. 70 J1. 7 Hz, 1 H), 7. 55 (dd, J 8. 0, 2. 0 Hz, 1 7. 38 J= 8. 3 Hiz, 1 7. 28 J= 12. 0 WO 02/053523 WO 02/53523PCT/JP01111083 Hz, 2 7. 16 j 7Hz, 1 7. 08 J 7Hz, I1H), 1. 66 4 1. 32 6 1. 26 6 H) Anal. Calcd for C 25
H,
6 0, 1/4H 2 0 C (79. 23 H 05 Found C (79. 43 H 12 2- 4-7Z 1 4 t /tmJ/" -U 22 OtD I 0 4L-A4-J 176 0 C 'H-NMR (400 MHz, DMSO-d 6 30 0 C) 7. 80 J 12. 2 Hz, 2 7. 57 (d, J= 3. 9 Hz, 1 7. 51 J= 3. 9 Hz, 1 7. 42 (dd, J= 8. 3, 2. 2 Hz, 1 7. 37 J 8. 6 Hz, 1 7. 24 J= 12. 0 Hz, 1 H1), 1. 66 4 H), 1. 29 6 1. 25 6 H) Anal. Calcd f or C 2 1H 26 1S 1 C (76. 89 H 71 Found C (76. 68 H 84 ~J24 t/4K0i Tp250 B+ I AICI 3 Br 1) ii-BuLi I ZnCi2 ci 63% 2) Pd(PPh 3 4 1 1-4 XII-1 21% 0 0 OMe NaH~/OH 62% XII-2 -9-z 2. 92 g(15.9 nimol) *74b#]2-2 m t)K LTA- %AMSO 3Cm Z±A U 6 WO 02/053523 PCT/JP01111083 iti XI-1 2. 88 g (63 SfL-ij~'jXII-1 'H-NMR (400 MHz, CDCL 3 7.90 J 2.0 Hz, 1 7.73 1 7.67 1 7.59 J 8.6 Hz, 1 7.41 (dd, J 9.4, 2.0 Hz, 1 1.76 4 1.38 6 1.38 (s, 6 H) 4LIM't10XII-1 796 mg (2.51 mmol) i-THF 5 ml -78 9C t\ n-? 72I 16 M 5 olution in hexane) 2. 35 ml 77 nmol) tjaLN U ft. 0) Mf -z;Lrtt 4 L K! n (I1) 342 m g (2.51 mmol) BTHF4 ml I 4) 4{l x i 1n 2KUT 1 R t 6 t- V I 1-4 415 mg 67 mmol) .RtiOPd(PPhl),496mg 08 mmol) ITHF 7 ml Lgb: t U t 2 *rI 5J(-jAjII hNM t- 2 N A"t ~i a (iE -jv) C.vrq 4L XII-2 198 mg (21 4 7'c* 4L-At-tXII-2 'H-NMIR (400 MHz, DMSO-d., 300C) 8.02 1 7.94 (s, 1 7.90 1 7.89 J 9.3 Hz, 1 7.75 (dd, J 12.9, 2.2 Hz, 1 7. 49-7.63 2 7. 17 J 12. 7 Hz, 1 7.11 J 10. 7 Hz, 1 3.90 3 1.74 4 1.37 12 H), 40-~1 iXII-2 150 mg 40 mmol) n- '7 ml U, 2 N 7}z'Ltt A 3 m 1 11 P 7 0 'C T' Tf U It. 3 0 3 r -7 L- t- T U 2 N 7 0~ L t t, A L~ 6 A, 5(E 3 t- V, M- tS -it, 4, -4 IRi~j L 0) IM: 7j" LYNA A L UN t' L L t- t, W4 k.7 #A fr \7 MgSO 4 j L7bc Li, 4L-t Tp250 lt)tt 89 mg (62 ~i~4l O 4L= i Tp250 t~iV F (9=kr n -YL- L) &W 192 OC ;H-NMR (400 MHz, DMSO-d 6 30 0 C) 8.03 1 7.95 1 7.90 1 7.89 (d, J 9. 5 Hz, 1 7.78 J It. 9 Hz, 2 7.60 (dd, J 8. 3, 1. 7 Hz, 1 WO 02/053523 PCT/JP01111083 7.33 J 11.7 Hz, 2 1.74 4 1.37 12 H) Anal. Calcd for C 2 6HZ6O 2 C (83.76 H (7.31 Found C (83. 49 H (7.52 AJ 25 JL-r=6-Tp2600~5t OEt ryOEt K 2 C0 3 SQ-AOEt PPA OEt 81% 63% S XIII-I XIII-2 1) n-BuLi/ ZnC[ 2 OMe NaOH
OH
2) Pd(PPh 3 4 /L-4 quant. y XII1-3 Tp 26 0 6, 7, 8-5z 1 Kt I 5, 8, 8-7 1 A f/'-2-'yJ7s 550 mg 50 mmol) LeDMF 4 ml 9 L gE tj 9 'jY7 691 mg 00 mmol) 7"t -7 lt bT/V~L5 0. 45 ml (591 minol, 3.00 mmol) ;kaU-Cn' *J 40, 140 -C,4*4 ft .L~/5 0 3 R k 7.l~r/L L U, 4LfKb XIII-1 677 mg (81 t4 4c1. XIII-1 'H-NMR (400 MHz, CDCL,) 7. 32 J 2. 0 Hz, 1 7. 21 J 8. 3 Hz, 1 7. 15 (dd, J 8. 3, 2. 2 Hz, 1 4.B4 J 5.6 Hz, 1 3.66 J 7.1 Hz, 2 3.54 J 7. 1 Hz, 2 3. 10 J 5. 6 Hz, 2 H1), 1. 66 4 1. 26 6 1. 6 1.19 J 7.1 Hz, 6 H), L-t1S XIII-2 673 mg 00 mmol) L bWc.>' 2. 5 ml -'Mr PPA g 90 0 CTN41LU-/.O 1 *rmj j 7PhP- ,z5L lC"tI W4 U, cj( A\MgSO 4 Z U- 7 WO 02/053523 PCT/JP01111083 Y ,/L3 5 7 n- 1 1 0) Tr$ L, 4L' XIII-2 309 mg (63 l) jo4f ~L-617 XII1-2 1 1-NMR (400 MHz, CDCL) 7.82 1 7.77 1 7.31 J 5.4 Hz, 1 7.22 J 4.9 Hz, 1 1.75 4 1.36 6 1.35 6 Hl) X't= JIII-2 192 mg 79 mmo1) THF 2 mli L -78 'C ir- C n-BuLi 1. 6 M k- 4VO 0. 74 ml 19 mmcl) ~ib~ 30 tL O, OD 4'{lM M 108 mg 79 mmo1) l- THF 2 ml I J ft V L il Ut'k 1 Ri-rMN, i- 11-2 149 mg 52 mmol) XZY Pd (PPh 3 4 30 mg 026 mmol) THF4ml U It t VD (LIN -M RT)JR1 t 3 RHO 7tu,-. WO 34 mg (15 C 8i' 4L- XIII-3 'H-NMR (400 MHz, CDCL) 7. 75 1 H), 7.72 1 7.71 (dd, J 12.7, 2.0 Hz, 111), 7.43 1 7.43 (dd, J 10.5, 2.0 Hz, 1 7.30 J 12.7 Hz, 1 6.82 J 10.7 Hz, 1 3.99 3 1.75 4 1.36 12 H) 0 {L'tf~j XIII-3 32 mg 085 mml) m 2 ml U, 2 N 7J1Y"fKY 9 1' A I m 1K)- P Z ME It J* At 3 3 J 2 N A MR K, L7', 'fi R Tp260 O)RttY t 32 mg (quant) V ft. 4L-h-AOj Tp260 (Wft J4E./-IV iJli~\ 172 0 C 'H-NMR (400 MHz, DMSO-d 6 30 C) 7. 91 (s, 1 7.81 J 12.0 Hz, 2 7.78 1 7.74 I 7.27 J 12.0 Hz, 2 1.69 4 1.32 12 H) Anal. Calcd for C 23
H
24 0,S, C (75. 79 H 64 Found C (75. 49 H 69 WO 02/053523 PCT/JP01111083 ~1 1: 4~~14L~~J~L W0 I4 3JZI X 10" M 0) H1X630 *750I-,1o 61-76440 4 tt~~m! 1i IJ~h~ 1-60 O-C Wft**\ 3a): L. 1 M10 f6l 0 N 0 1U' WO 02/053523 WO 02/53523PCT/JP01111083 1 x 10-7 M HX630 tii-irz Tp 10 Tp2O Tp22 Tp 50 Tp8O Tp82 Tp84 Tp88 Tp93 TpA14 Tp 141 Tp 145 Tp146 Tp 149 Tp 150 Tp155 -8 0. 6 6. 8 2. 1 2. 8 1. 3 1. 3 1. 6 0. 8 7 0. 5 0. 7 0. 9 0. 7 0. 6 0. 5 65 2. 2 73 3. 6 1.4 1. 5 2. 7 -7 0. 5 2. 9 1.8 2.4 1. 5 0. 9 2. 8 1. 3 26 1. 2 5 1.2 0. 9 0. 8 0. 5 73 3. 3 76 2. 2 4 5.4 24 -6 13 3. 3 2. 7 18 1. 2 2. 3 5. 1 2. 1 21 1.4 26 46 67 9 0. 3 14 6.4 70 69 40 60 62. 5 2. 2 82 1. 9 15 2. 6 1. 5 3. 6 0. 8 89 4. 1 82 66 3. 5 9 68 -7 1.2 2. 9 3. 7 3. 3 2. 3 2. 5 21. 2 85 7 89 14 2. 1 0. 8 0. 5 93 7 75 91 85 80 89 -6 5.6 2.4 78 2 37. 8 79 42 62 43 1.7 66 84 77 83 78- Tp160 18. 5 34. 4 32 Tpl7O Tp175 TP 180 Tpl9O Tp200 Tp2 10 Tp260 0. 8 1. 2 0. 5 32 14 6 66 20 81 84 0. 5 2.3 3 2 33 2. 7 2.6 33 77 90 77 95 64 91 91 91 84 79 91 83 67 J7XtU F ",Z7 MR

Claims (7)

1. A medicament comprising the compound represented by the following general Z formula or a salt thereof ON R 1 cI0 00 R 4 cO IN ci (I) C] 5 wherein R 2 R 3 and R 4 independently represent hydrogen atom, a alkyl 0 group, said alkyl group may be substituted, or a alkoxyl group, and when R 2 and R 3 are adjacent to each other, they may combine together with carbon atoms of the phenyl group to which R 2 and R 3 bind to form a 5- or 6-membered ring, said ring may have one or more C,-C 4 alkyl groups or one condensed benzene ring which may. have one or more substituents on the ring; the ring represented by Ar represents an aryl ring; X represents a single bond, -CON(Rs)-, (wherein R 5 represents hydrogen atom or a alkyl group), wherein n represents an integer of 1 to 3, and R 6 represents hydrogen atom or a alkyl group, -N(R T CON(R 8 R 7 and R 8 represent hydrogen atom or a C,-C alkyl group, -SO 2 N(R 9 R 9 represents hydrogen atom or a alkyl group, -N(R 1 0 R' 0 represents hydrogen atom, a alkyl group, or a C,-C acyl group, a Ci-C, alkylene group, said alkylene group may contain one or more unsaturated bonds or a cyclic structure, an aryldiyl group; Y represents hydrogen atom, -OR 11 R 1 represents hydrogen atom, a Cl-C, alkyl group, or a C,-C 6 acyl group, -NHR' 2 R' 2 represents hydrogen atom, a alkyl group, a acyl group, or amino group, or a halogen atom.
2. The medicament of claim 1 wherein R 4 is hydrogen atom or a alkyl group, Y is hydrogen atom, hydroxyl group, a C,-Ce alkoxyl group, hydrazino group, or a halogen atom.
3. A method for treating leukemia, comprising administering a pharmaceutical composition of the medicament according to claim 2 in a therapeutically effective amount. I: COMS ID No: ARCS-170595 Received by IP Australia: Time 16:33 Date 2007-11-29 29/11/207 14:54 COLLISON CO FDELFIDE 0262837999 N0.899 o009
4. A pharmaceutical composition comprising the compound or a physiologically acceptable salt thereof according to claim 2. A method for treating leukemia, comprising administering a pharmaceutical composition according to claim 5 in a therapeutically effective amount.
6. The medicament of claim 1 wherein the compound or salt thereof according to claim 1, is a compound or salt thereof of the following formula: wherein R 1 and R 5 are hydrogen.
8. A pharmaceutical composition comprising the compound or a physiologically acceptable salt thereof according to claim 7.
9. A method for treating leukemia, comprising administering a pharmaceutical composition according to claim 7 in a therapeutically effective amount. COMS ID No: ARCS-170595 Received by IP Australia: Time 16:33 Date 2007-11-29
AU2002222682A 2000-12-26 2001-12-18 Tropolone Derivatives Ceased AU2002222682B8 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2000394338 2000-12-26
JP2000-394338 2000-12-26
PCT/JP2001/011083 WO2002053523A1 (en) 2000-12-26 2001-12-18 Tropolone derivative

Publications (3)

Publication Number Publication Date
AU2002222682A1 AU2002222682A1 (en) 2003-01-23
AU2002222682B2 AU2002222682B2 (en) 2007-12-13
AU2002222682B8 true AU2002222682B8 (en) 2008-05-29

Family

ID=18859983

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2002222682A Ceased AU2002222682B8 (en) 2000-12-26 2001-12-18 Tropolone Derivatives

Country Status (8)

Country Link
US (1) US7259187B2 (en)
EP (1) EP1357104A4 (en)
JP (1) JPWO2002053523A1 (en)
KR (1) KR20030077558A (en)
CN (1) CN1247511C (en)
AU (1) AU2002222682B8 (en)
CA (1) CA2432409A1 (en)
WO (1) WO2002053523A1 (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1733722A4 (en) * 2004-03-10 2010-07-14 Res Found Itsuu Lab Memory fixation accelerator
WO2007037188A1 (en) * 2005-09-27 2007-04-05 Sapporo Medical University Pharmaceutical for prevention and treatment of ophthalmic disease induced by increase in vasopermeability
US7427316B2 (en) * 2005-12-30 2008-09-23 E.I. Du Pont De Nemours And Company Tropolone complexes as wood preservatives
US7540906B2 (en) * 2005-12-30 2009-06-02 E.I. Du Pont De Nemours & Company Metal salts of hydrolyzed olefin/maleic anhydride copolymers and their use as wood preservatives
US7462227B2 (en) * 2005-12-30 2008-12-09 E.I. Du Pont De Nemours And Company Ibuprofen complexes as wood preservatives
US7497901B2 (en) * 2005-12-30 2009-03-03 E. I. Dupont De Nemours And Company Tungstate and molybate wood preservatives
EP2513057B1 (en) * 2009-12-14 2013-09-04 Merck Patent GmbH Sphingosine kinase inhibitors
JP2013514287A (en) * 2009-12-17 2013-04-25 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング Inhibitors of sphingosine kinase
WO2013038931A1 (en) * 2011-09-12 2013-03-21 壽製薬株式会社 Method of producing 2-oxo-2h-cyclohepta[b]furan analogue
JP7503310B2 (en) * 2018-04-13 2024-06-20 ザ ボード オブ トラスティーズ オブ ザ ユニヴァーシティ オブ イリノイ Hinokitiol analogues, their preparation methods and pharmaceutical compositions
CN109776357A (en) * 2018-08-29 2019-05-21 湖北工业大学 A kind of micromolecular inhibitor containing tropolone and the application in inhibition ornithine decarboxylase (ODC)
EP4045477A4 (en) * 2019-10-16 2024-09-25 Kinesid Therapeutics Inc Tropolone derivatives and tautomers thereof for iron regulation in animals
WO2021076945A1 (en) * 2019-10-16 2021-04-22 Ambys Medicines, Inc. Tropolone derivatives and tautomers thereof for iron regulation in animals

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3391133A (en) * 1965-08-02 1968-07-02 Research Corp Methacrylate esters of tropolones
US3424841A (en) * 1966-01-28 1969-01-28 Research Corp Method of inhibiting bacteria with germicidal tropolone polymer compositions
JPS5750934A (en) * 1980-09-16 1982-03-25 Sankyo Co Ltd Preparation of tropone having double bond in side chain
WO1998007708A1 (en) * 1996-08-21 1998-02-26 Pharmacia & Upjohn Company Isoxazoline derivatives useful as antimicrobials

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4314705Y1 (en) 1965-09-09 1968-06-20
FR2080201A6 (en) 1970-02-26 1971-11-12 Wendel Sidelor
JPS6176440A (en) 1984-09-19 1986-04-18 Koichi Shiyudo Benzoic acid derivative
JPS6122047A (en) 1984-07-07 1986-01-30 Koichi Shiyudo Benzoic acid derivative
JPS61215341A (en) * 1985-03-20 1986-09-25 Masatoshi Yamato Production of tropolone derivative and use as antitumor agent
US5235076A (en) 1991-05-28 1993-08-10 University Of Hawaii Azulenic retinoid compounds, compositions and methods
WO1995004036A1 (en) 1993-01-11 1995-02-09 Ligand Pharmaceuticals Inc. Compounds having selective activity for retinoid x receptors, and means for modulation of processes mediated by retinoid x receptors

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3391133A (en) * 1965-08-02 1968-07-02 Research Corp Methacrylate esters of tropolones
US3424841A (en) * 1966-01-28 1969-01-28 Research Corp Method of inhibiting bacteria with germicidal tropolone polymer compositions
JPS5750934A (en) * 1980-09-16 1982-03-25 Sankyo Co Ltd Preparation of tropone having double bond in side chain
WO1998007708A1 (en) * 1996-08-21 1998-02-26 Pharmacia & Upjohn Company Isoxazoline derivatives useful as antimicrobials

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
Aust J Chem, 1997, vol 50, pp 115-122 *
Biochimica et Biophysica Acta, 1994, vol 1208, 127-135 *
Bull Chem Soc Jpn, 1976, vol 49, no 3, pp 831-832 *
Chem Lett, 1977, pp 1505-1508 *
Mutation Research, 1985, vol 157, pp 29-37 *
Yakagaku Zasshi, 1988, vol 108, no 8, pp 754-757 *

Also Published As

Publication number Publication date
EP1357104A1 (en) 2003-10-29
WO2002053523A1 (en) 2002-07-11
US7259187B2 (en) 2007-08-21
CN1247511C (en) 2006-03-29
AU2002222682B2 (en) 2007-12-13
US20040082550A1 (en) 2004-04-29
CA2432409A1 (en) 2002-07-11
EP1357104A4 (en) 2004-07-28
KR20030077558A (en) 2003-10-01
CN1491197A (en) 2004-04-21
JPWO2002053523A1 (en) 2004-04-30

Similar Documents

Publication Publication Date Title
AU2002222682B8 (en) Tropolone Derivatives
Bräse et al. Solid-phase synthesis of urea and amide libraries using the T2 triazene linker
ES2333445T3 (en) DERIVATIVES OF 2-PHENYLPROPIONIC ACID AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM.
Artamonov et al. Synthesis of Trifluoromethyl-Substituted 3-Azabicyclo [n. 1.0] alkanes: Advanced Building Blocks for Drug Discovery.
Wienand et al. Reactions of Fischer carbene complexes with electron-deficient olefins: scope and limitations of this route to donor-acceptor-substituted cyclopropanes
BRPI0706610A2 (en) nicotinically acetylcholine alpha 7 receptor modulators and therapeutic uses of these
Hu et al. Macrocyclic inhibitors for peptide deformylase: a structure− activity relationship study of the ring size
Ma et al. General route to 2, 4, 5-trisubstituted piperidines from enantiopure β-amino esters. Total synthesis of Pseudodistomin B triacetate and Pseudodistomin F
Smith et al. Variation in the site of lithiation of 2-(2-methylphenyl) ethanamine derivatives
Straker et al. Exploiting rhodium-catalysed ynamide hydroacylation as a platform for divergent heterocycle synthesis
Zanakhov et al. Diazo Strategy for Intramolecular Azirine Ring Expansion: Rh (II)-Catalyzed Synthesis of 2-Hydroxy-3-oxo-2, 3-dihydro-1 H-pyrrole-2-carboxylates
Yarmolchuk et al. Synthesis of β-fluoro-β-proline
Huang et al. Phosphine-mediated domino reactions of phthalimidomalonates with allenoates or but-2-ynoate: facile entry into highly functionalized pyrroloisoindolinone derivatives
Rozentsveig et al. Amidine derivatives of α-arylglycines from N-(1-aryl-2, 2, 2-trichloroethyl) amides of arenesulfonic acids and secondary amines
CN111763148A (en) Alkynyl cyclopentene derivative containing trifluoromethyl and preparation method and application thereof
Garcia et al. Leveraging the 1, 3-azadiene-anhydride reaction for the synthesis of functionalized piperidines bearing up to five contiguous stereocenters
Uddin et al. Brønsted acid-catalyzed C–C bond forming reaction for one step synthesis of oxazinanones
Dang et al. One-pot synthesis of pyrazole-5-carboxylates by cyclization of hydrazone 1, 4-dianions with diethyl oxalate
Nimje et al. Synthesis of differentially protected azatryptophan analogs via Pd2 (dba) 3/XPhos catalyzed Negishi coupling of N-Ts azaindole halides with zinc derivative from Fmoc-protected tert-butyl (R)-2-amino-3-iodopropanoate
CN110256443A (en) A kind of indole derivatives and preparation method thereof
Lee et al. Structural modification of an orally active thrombin inhibitor, LB30057: replacement of the D-pocket-binding naphthyl moiety
Song et al. A novel one-step synthesis of 2-substituted 6-azaindoles from 3-amino-4-picoline and carboxylic esters
Sampson et al. Oxidative deprotection of diphenylmethylamines
DeBruin et al. A new route to N-monosubstituted thioamides utilizing phosphoramidothionates as reagents for the thioamidation of carboxylic acids
Lyutenko et al. Regioselective reactions of β-aminovinyl trifluoromethyl ketones with tosyl isocyanate

Legal Events

Date Code Title Description
PC1 Assignment before grant (sect. 113)

Owner name: RESEARCH FOUNDATION ITSUU LABORATORY

Free format text: FORMER APPLICANT(S): KAGECHIKA, HIROYUKI; RESEARCH FOUNDATION ITSUU LABORATORY

FGA Letters patent sealed or granted (standard patent)
TH Corrigenda

Free format text: IN VOL 21, NO 49, PAGE(S) 5680 UNDER THE HEADING APPLICATIONS ACCEPTED -NAME INDEX UNDER THE NAME RESEARCH FOUNDATION ITSUU LABORATORY, APPLICATION NO. 2002222682, UNDER INID (54), CORRECT THE TITLE OF THE INVENTION TO TROPOLONE DERIVATIVES

MK14 Patent ceased section 143(a) (annual fees not paid) or expired